HGVS | Genome Assembly |
---|---|
NC_000008.11:g.8864863G= , CM000670.2:g.8864863G= | GRCh38 |
NC_000008.10:g.8722373G= , CM000670.1:g.8722373G= | GRCh37 |
NC_000008.9:g.8759783G= | NCBI36 |
NG_009444.1:g.33759C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000276282.7:c.2998+25198C= MANE Select | ENSP00000276282.6:n.2998+25198C= | |
ENST00000276282.6:c.2998+25198C= | ENSP00000276282.6:n.2998+25198C= | |
NM_004225.2:c.2998+25198C= | NP_004216.2:n.2998+25198C= | |
XR_246634.2:n.3534+25198C= | ||
XM_024447330.1:c.2998+25198C= | XP_024303098.1:n.2998+25198C= | |
NM_004225.3:c.2998+25198C= MANE Select | NP_004216.2:n.2998+25198C= |